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Items: 18

1.

nsv3894905

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MARVELD1
,
ZFYVE27
,
SFRP5
Location information:
Clinical significance:
Uncertain significance
ID:
48458260
variant
2.

nsv7137209

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-12P
,
RNU1-65P
,
AGAP6
,
RPL15P13
,
LHPP
,
MTCO2P23
,
CHAT
,
LINC02935
,
XRCC6P1
,
MIR548F1
,
ENTPD1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55356054
variant
3.

nsv3920295

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EIF2S2P3
,
CYP17A1-AS1
,
MTND4P19
,
PRLHR
,
LBX1
,
ABRAXAS2
,
KLLN
,
WARS2P1
,
DUX4L28
,
PTPRE
,
LOC107984252
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483650
variant
4.

nsv3911437

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLF2
,
CUTC
,
ARHGAP19-SLIT1
,
LINC01475
,
PDLIM1
,
LCOR
,
ZFYVE27
,
TWNK
,
RPL7P36
,
EXOSC1
,
RPL12P27
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474792
variant
5.

nsv3894877

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNY3P12
,
ANKRD2
,
ZFYVE27
,
IDE
,
COX15
,
RPL12P27
,
SLIT1
,
ALDH18A1
,
MTND4P20
,
LOC107984256
,
CUTC
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458232
variant
7.

nsv3906389

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100419870
,
LOC102724439
,
LOC105378313
,
ELOVL3
,
MIR936
,
YWHAZP5
,
RN7SL394P
,
LOC105376398
,
PWWP2B
,
MIR4675
,
DUSP8P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469744
variant
8.

nsv3891157

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AGAP14P
,
LOC100505502
,
LINC01514
,
LOC105378549
,
SIRT1
,
UROS
,
LOC105378443
,
KSR1P1
,
LOC105378314
,
LINC02663
,
LOC100130881
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454512
variant
9.

nsv3902271

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ANXA11
,
EDRF1-DT
,
TSPAN14
,
NUTM2A-AS1
,
LOC105378549
,
LINC02646
,
KCNMA1
,
RN7SKP196
,
LOC105376357
,
LOC105378552
,
GLRX3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465626
variant
10.

nsv3891958

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TUBB8
,
PPP2R2D
,
NRAP
,
LOC105376475
,
LOC101928834
,
LOC105376372
,
ITPRIP-AS1
,
LINC00702
,
LIPF
,
CASC2
,
RNU6-1090P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455313
variant
11.

nsv7137211

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EXOC6
,
VCL
,
EBAG9P1
,
LOC105378573
,
LINC01264
,
LINC02627
,
MED6P1
,
ALDH7A1P4
,
MIR4675
,
RPS27P18
,
SAMD8
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55356056
variant
12.

nsv3905489

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378476
,
SMC3
,
EIF2S2P3
,
PDZD8
,
PRDX3
,
TBC1D12
,
FGF8
,
HSPA12A-AS1
,
LINC00601
,
CYP17A1-AS1
,
SPCS2P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468844
variant
13.

nsv3890046

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UROS
,
KCNK18
,
LOC105378549
,
C10orf88B
,
LINC02646
,
MIR548E
,
GLRX3
,
EEF1AKMT2
,
SUFU
,
CHST15
,
RN7SL749P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453401
variant
14.

nsv3909942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102723665
,
SFR1
,
RNU6-839P
,
PNLIP
,
DNTT
,
MIR4685
,
ARL3
,
MIR3158-1
,
RPL7P35
,
LOC105378492
,
LOC107984265
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473297
variant
15.

nsv3907664

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SHOC2
,
FAM245B
,
LINC00865
,
RN7SL840P
,
LOC107984179
,
DNMBP-AS1
,
RNY4P26
,
NT5C2
,
FAM149B1
,
RPS15AP5
,
PPP3CB-AS1
,
See more...
Location information:
Clinical significance:
drug response
ID:
48471019
variant
16.

nsv3894450

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HPS1
,
LOC112268063
,
RRP12
,
MED6P1
,
WNT8B
,
LOC105378447
,
LOC105378424
,
LOC105378401
,
LOC107984263
,
ARL3
,
TLL2
,
See more...
Location information:
Clinical significance:
drug response
ID:
48457805
variant
17.

nsv3893201

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SFRP5
,
LOC107984260
,
MARVELD1
,
PI4K2A
,
AVPI1
,
GOLGA7B-DT
,
ZFYVE27
Location information:
Clinical significance:
Uncertain significance
ID:
48456556
variant
18.

nsv7093904

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ABCC2
,
LBX1-AS1
,
LOC107984265
,
LOC105378460
,
HIF1AN
,
FBXW4
,
SFRP5
,
ARL5AP2
,
MIR146B
,
LDB1
,
LINC01514
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55274093
variant
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